标题
Mitochondrial diseases and epilepsy
作者
关键词
-
出版物
EPILEPSIA
Volume 53, Issue -, Pages 92-97
出版商
Wiley
发表日期
2012-09-05
DOI
10.1111/j.1528-1167.2012.03618.x
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Mitochondrial disease and epilepsy
- (2012) SHAMIMA RAHMAN DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
- Defects in mitochondrial DNA replication and human disease
- (2011) William C. Copeland CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY
- Epileptic Seizures in Infants and Children With Mitochondrial Diseases
- (2011) Hsiu-Fen Lee et al. PEDIATRIC NEUROLOGY
- Mitochondrial DNA mutations affect calcium handling in differentiated neurons
- (2010) Andrew J. Trevelyan et al. BRAIN
- Localized cerebral energy failure in DNA polymerase gamma-associated encephalopathy syndromes
- (2010) Charalampos Tzoulis et al. BRAIN
- Gamma oscillations in the hippocampus require high complex I gene expression and strong functional performance of mitochondria
- (2010) Oliver Kann et al. BRAIN
- Epileptic phenotypes in children with respiratory chain disorders
- (2010) Sandra El Sabbagh et al. EPILEPSIA
- Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005-2009
- (2010) Anne T. Berg et al. EPILEPSIA
- Acute, Reversible Axonal Energy Failure During Stroke-Like Episodes in MELAS
- (2010) M. A. Farrar et al. PEDIATRICS
- Mutations in the mitochondrial glutamate carrierSLC25A22in neonatal epileptic encephalopathy with suppression bursts
- (2009) F Molinari et al. CLINICAL GENETICS
- The ketogenic diet and epilepsy
- (2009) Do Young Kim et al. CURRENT OPINION IN CLINICAL NUTRITION AND METABOLIC CARE
- Pathogenic Mitochondrial DNA Mutations Are Common in the General Population
- (2008) Hannah R. Elliott et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Mitochondrial Disorders in the Nervous System
- (2008) Salvatore DiMauro et al. Annual Review of Neuroscience
- POLG1 mutations cause a syndromic epilepsy with occipital lobe predilection
- (2008) B. A. Engelsen et al. BRAIN
- Epilepsy and respiratory chain defects in children with mitochondrial encephalopathies
- (2008) Divya Khurana et al. EPILEPSIA
- Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with neuronal complex I defect and mtDNA depletion
- (2008) A. H. Hakonen et al. HUMAN MOLECULAR GENETICS
- Partial inhibition of complex I activity increases Ca2+-independent glutamate release rates from depolarized synaptosomes
- (2008) Sen M. Kilbride et al. JOURNAL OF NEUROCHEMISTRY
- Serial Diffusion Imaging in a Case of Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes
- (2008) Charalampos Tzoulis et al. STROKE
- Prevalence of mitochondrial DNA disease in adults
- (2007) Andrew M. Schaefer et al. ANNALS OF NEUROLOGY
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationCreate your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create Now